Method and system for wound care

ABSTRACT

In one aspect, the present invention relates to a wound-care assembly The wound-care assembly includes a base layer. A film layer is operatively coupled to the base layer and a fluid conductor is in fluid communication with a wound and a vacuum source. The wound-care assembly further includes a fiber-optic patch comprising a plurality of fiber-optic strands. The fiber-optic strands are pressed into contact with an interior surface of the wound by the fluid conductor. The fiber-optic patch provides ultraviolet light to the wound and the relative vacuum is applied to the wound via the vacuum source and the fluid conductor.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application claims priority to, and incorporates by reference for any purpose the entire disclosure of, U.S. Provisional Patent Application No. 61/902,455, filed Nov. 11, 2013.

BACKGROUND

Field of the Invention

The present invention relates to a wound care method and system with one or both of vacuum-light therapy, pulsed radio frequency (“RF”), and oxygenation, and more particularly, but not by way of limitation, to adaptive wound-care patch capable of being utilized in a variety of wound locations where one or both of vacuum-light therapy, pulsed radio frequency (“RF”), and oxygenation may be applied thereto.

History of the Related Art

An important aspect of patient treatment is wound care. Medical facilities are constantly in need of advanced technology for the cleaning and treatment of skin wounds. The larger the skin wound, the more serious the issues are of wound closure and infection prevention. The rapidity of the migration over the wound of epithelial and subcutaneous tissue adjacent the wound is thus critical. Devices have been developed and/or technically described which address certain aspects of such wound healing. For example, U.S. Pat. No. 6,695,823 to Lina et al. (“Lina”) describes a wound therapy device that facilitates wound closure. A vacuum pump is taught for collecting fluids from the wound. WO 93/09727 discloses a solution for wound drainage by utilizing negative pressure over the wound to promote the above references migration of epithelial and subcutaneous tissue over the wound.

In other embodiments, wound treatment is performed using light therapy. For example, U.S. Pat. No. 7,081,128 to Hart et al. (“Hart”) describes a method of treating various medical conditions such as, for example, joint inflammation, edema, etc., utilizing an array of Light Emitting Diodes contained on a flexible substrate that may be wrapped around an anatomical feature of the human body. U.S. Pat. No. 6,596,016 to Vreman et al. (“Vreman”) discloses a phototherapy garment for an infant having a flexible backing material, a transparent liner, and a flexible printed circuit sheet containing surface-mounted LEDs. The LEDs preferably emit high-intensity blue light, suitable for the treatment of neonatal hyperbilirubinemia. The device may include a portable power supply.

In other embodiments, wound treatment is performed using oxygen. The use of oxygen for the treatment of skin wounds has been determined to be very beneficial in certain medical instances. The advantages are multitudinous and include rapidity in healing. For this reason, systems have been designed for supplying high concentration of oxygen to wound sites to facilitate the healing process. For example, U.S. Pat. No. 5,578,022 to Scherson et al. (“Scherson”) teaches an oxygen producing bandage and method. One of the benefits cited in Scherson is the ability to modulate a supply of concentrated hyperbaric oxygen to skin wounds. Although oxygen is beneficial in direct application of predetermined dosages to skin wounds, too much oxygen can be problematic. Oxygen applied to a wound site can induce the growth of blood vessels for stimulating the growth of new skin. Too much oxygen, however, can lead to toxic effects and the cessation of healing of the wound. It would be an advantage, therefore, to maximize the effectiveness of oxygen applied to a wound area by enhancing the absorption rate of oxygen into the skin and tissue fluids. By enhancing the absorption rate of the oxygen in the wound, less exposure time and concomitantly fewer toxic side effects to the endothelial cells surrounding the wound, such as devasculation, occurs. It would be a further advantage, therefore, to utilize existing medical treatment modalities directed toward other aspects of patient therapy to augment oxygenation for wound care.

SUMMARY

The present invention relates generally to a wound care method and system with one or both of vacuum-light therapy, pulsed radio frequency (“RF”), and oxygenation, and more particularly, but not by way of limitation, to adaptive wound-care patch capable of being utilized in a variety of wound locations where one or both of vacuum-light therapy, pulsed radio frequency (“RF”), and oxygenation may be applied thereto.

In one aspect, the present invention relates to a wound-care assembly The wound-care assembly includes a base layer. A film layer is operatively coupled to the base layer and a fluid conductor is in fluid communication with a wound and a vacuum source. The wound-care assembly further includes a fiber-optic patch comprising a plurality of fiber-optic strands. The fiber-optic strands are pressed into contact with an interior surface of the wound by the fluid conductor. The fiber-optic patch provides ultraviolet light to the wound and the relative vacuum is applied to the wound via the vacuum source and the fluid conductor.

In another aspect, the present invention relates to a method of utilizing a wound-care assembly. The method includes applying a fiber-optic patch to a wound. The fiber-optic patch is pressed into contact with an inner surface of the wound via a fluid conductor. The fluid conductor and the fiber-optic patch are secured to the wound. A vacuum applicator is applied to and secured to the fluid conductor. Ultraviolet light is applied to the wound via the fiber-optic patch and a relative vacuum is applied to the wound via the fluid conductor.

BRIEF DESCRIPTION OF THE DRAWINGS

For a more complete understanding of the present invention and for further objects and advantages thereof, reference may now be had to the following description taken in conjunction with the accompanying drawings in which:

FIG. 1A is a top view of a wound-care patch according to an exemplary embodiment;

FIG. 1B is an exploded view of the wound-care patch of FIG. 1A according to an exemplary embodiment;

FIG. 1C is a perspective view of the wound-care patch of FIG. 1A according to an exemplary embodiment;

FIG. 2 is a bottom view of the wound-care patch of FIG. 1 according to an exemplary embodiment;

FIG. 3 is a flow diagram of a method for using the wound-care patch of FIG. 1 according to an exemplary embodiment;

FIG. 4A is a top view of a package containing a wound-care assembly according to an exemplary embodiment;

FIG. 4B is a an exploded view of the wound-care assembly of FIG. 4A;

FIG. 5A is a bottom view of the wound-care assembly of FIG. 4 applied to a foot according to an exemplary embodiment;

FIG. 5B is a top view of the wound-care assembly of FIG. 4 applied to a foot according to an exemplary embodiment; and

FIG. 6 is a flow diagram of a method for using the wound-care patch of FIG. 4 according to an exemplary embodiment.

DETAILED DESCRIPTION

Various embodiments of the present invention will now be described more fully with reference to the accompanying drawings. The invention may, however, be embodied in many different forms and should not be construed as limited to the embodiments set forth herein.

FIG. 1 is a top view of a wound-care patch 100. The wound-care patch 100 includes a base layer 102 that is coupled to a film layer 104. In a typical embodiment, the base layer 102 is constructed of a sterile, ethylyne-oxide, biocompatible material. The film layer 104 is, in a typical embodiment, constructed from, for example, medical grade polyurethane. A peripheral edge 106 of the film layer 104 is secured to a corresponding edge of the base layer 102 through a process such as, for example, welding. Connection of the film layer 104 to the base layer 102 creates a seal around the peripheral edge 106, which seal prevents leakage of fluid therefrom. A fluid port 114 is formed in the film layer 104.

Still referring to FIG. 1, a fluid conductor 108 is disposed between the base layer 102 and the film layer 104. In a typical embodiment, the fluid conductor 108 is flexible, absorptive, and constructed of, for example, medical grade foam. The fluid conductor includes a wound-treatment portion 110 disposed proximate a wound (not shown in FIG. 1) and a straw portion 112 that fluidly couples the wound-treatment portion 110 to the fluid port 114. In a typical embodiment, the fluid conductor 108 transmits fluids such as, for example, liquids or gases, from the wound to the fluid port 114 and, thus, allows a vacuum to be applied to the wound via the fluid port 114. In addition, the straw portion 112 facilitates placement of the fluid port 114 at a location removed from the wound. Such an arrangement is beneficial if, for example, space constraints do not allow the fluid port 114 to be placed near the wound.

Still referring to FIG. 1, a fiber-optic cable 116 is coupled to the wound-care patch 100. A plurality of fiber-optic strands 118 extend from the fiber-optic cable 116. The fiber-optic strands are disposed between the base layer 102 and the film layer 104 and are arranged in a generally flat, side-by-side configuration. The fiber-optic strands 118 are disposed beneath the fluid conductor 108.

FIG. 1B is an exploded view of the wound-care patch 100. FIG. 1C is a perspective view of the wound-care patch 100. FIG. 2 is a bottom view of the wound-care patch 100. Referring to FIGS. 1B-2 together, a window 120 is formed in a bottom face of the base layer 102. The fiber-optic strands 118 extend across the window 120. The wound-treatment portion 110 of the fluid conductor 108 (shown in FIG. 1A) is disposed over the window 120 above the fiber-optic strands 118. In a typical embodiment, the wound-care patch 100 is arranged such that the window 120 is positioned over the wound. A mesh 121 extends across the window 120 below the fiber-optic strands 118. In a typical embodiment, the mesh 121 prevents adhesion of wound tissue to either the fiber-optic strands 118 or the fluid conductor 108. A biocompatible skin adhesive (not shown) such as, for example, Tegaderm™, manufactured by 3M Company (hereinafter “Tegaderm”), is used to secure the edges of the wound-care patch 100 to skin surrounding the wound.

During operation, a vacuum pump (not explicitly shown) is coupled to the fluid port 114. Such an arrangement allows a relative vacuum to be applied to the wound via the fluid conductor 108. In addition, a source of ultra-violet light (not explicitly shown) is coupled to the fiber-optic strands 118. The ultra-violet light is emitted from the fiber-optic strands 118 into the wound. The ultraviolet light emitted from the fiber-optic strands 118 may be modulated to create various patterns of light, different intensities of light, and different durations of light such as, for example, pulsed emission of ultraviolet light. The ultraviolet light is capable of penetrating through several layers of skin to destroy infectious bacteria. According to exemplary embodiments, the ultraviolet light from fiber-optic strands 118 destroys a wide variety of microorganisms such as, for example, bacteria which causes skin infections. In addition, the ultraviolet light from the fiber-optic strands 118 improves wound healing along with cell and bone growth. Furthermore, the use of ultraviolet light in light therapy is safe, non-invasive, drug-free and therapeutic.

Still referring to FIGS. 1C-2, in various embodiments, a therapeutic agent, such as, for example, concentrated oxygen may be applied to the wound site via the port 114. In such embodiments, the port 114 may include two parallel lumen couplings to facilitate alternating application of the therapeutic agent and the relative vacuum. In various embodiments, the therapeutic agent may be thermally augmented prior to application to the wound area. In other embodiments, the therapeutic agent is not thermally augmented. Still referring to FIGS. 1C-2, in various embodiments, a radio frequency (“RF”) antenna 122 is disposed around the window 120. In a typical embodiment, the RF antenna 122 comprises a wire 124. The wire 124 extends around a perimeter of the window 120. In a typical embodiment, the wire 124 is disposed such that, during use, the wire 124 is in close proximity to the wound. In various embodiments, the wire 124 is insulated to reduce risk of electric shock to a patient.

Still referring to FIGS. 1C-2, during operation, a pulsed radio-frequency (“RF”) signal having a pulse frequency on the order of, for example 27 MHz, is transmitted to the RF antenna 122. In a typical embodiment, an amplitude of the pulsed RF signal is on the order of, for example, a fraction of a Watt. Such an amplitude is below a threshold where federal licensing is typically required. The RF antenna 122 receives the pulsed RF signal from a radio-frequency source and transmits the pulsed RF signal to a region in close proximity to the wound. Exposing the wound to the pulsed RF signal has been shown to be beneficial to healing by encouraging intracellular communication. In particular, pulsed RF signals have been shown to stimulate cellular bonding, and metabolism.

FIG. 3 is a flow diagram of a process 300 for using the wound-care patch 100. The process 300 begins at step 302. At step 304, the wound-care patch 100 is applied to a wound. At step 306, a biocompatible skin adhesive is used to secure the edges of the wound care patch 100 to a patient's skin surrounding the wound. At step 308, the fluid port 114 is coupled to a vacuum source and the fiber-optic cable 116 is connected to an ultraviolet light source. At step 310, a relative vacuum is applied to the fluid port 114. The relative vacuum is transmitted to the wound via the fluid conductor 108. In various embodiments, the relative vacuum facilitates removal of undesirable tissues from the wound such as, for example, dead tissue and foreign contaminants. In addition, the relative vacuum draws out fluid from the wound thereby increasing blood flow into the wound area. At step 312, ultraviolet light is supplied to the wound via the fiber-optic cable 116 and the fiber-optic strands 118. In a typical embodiment, the ultraviolet light is supplied to the wound area simultaneous with the application of the relative vacuum. In other embodiments, at least one of the ultraviolet light and the relative vacuum may be modulated or applied in various patterns and, thus, may not be simultaneous. The process 300 ends at step 314.

FIG. 4A is a top view of a package 401 containing a wound-care assembly 400. FIG. 4B is an exploded view of the wound-care assembly 400. Referring to FIGS. 4A and 4B together, the wound-care assembly 400 includes a fiber-optic patch 402. The fiber-optic patch includes a plurality of fiber-optic strands 404. In a typical embodiment, the plurality of fiber-optic strands 404 are arranged in a generally flat side-by-side arrangement. The plurality of fiber-optic strands 404 are optically coupled to a fiber-optic cable 406. In a typical embodiment, the fiber-optic cable 406 is optically connectable to a source of ultraviolet light. The wound-care assembly 400 further includes a vacuum applicator 408. The vacuum applicator 408 includes a base layer 412 and a film layer 414. A fluid port 410 is formed in the film layer 414. A fluid conductor 416 is disposed beneath the fluid port 410 between the film layer 414 and the base layer 412. In a typical embodiment, the fluid conductor 416 is flexible, absorptive, and constructed of, for example, medical grade foam. In a typical embodiment, the fluid port 410 is connectable to a vacuum source. In a typical embodiment, the package 401 maintains the wound-care assembly in a sterile environment until use.

Still referring to FIGS. 4A and 4B, an RF layer 403 is disposed above the fiber-optic patch 402. The RF layer 403 includes an antenna 405 embedded therein. In a typical embodiment, the antenna 405 forms a loop around the wound. During operation, a pulsed radio-frequency (“RF”) signal having a pulse frequency on the order of, for example 27 MHz, is transmitted to the antenna 405. In a typical embodiment, an amplitude of the pulsed RF signal is on the order of, for example, a fraction of a Watt. Such an amplitude is below a threshold where federal licensing is typically required. The antenna 405 receives the pulsed RF signal from a radio-frequency source and transmits the pulsed RF signal to a region in close proximity to the wound. Exposing the wound to the pulsed RF signal has been shown to be beneficial to healing by encouraging intracellular communication. In particular, pulsed RF signals have been shown to stimulate cellular bonding, and metabolism.

FIG. 5A is a bottom view of the wound-care assembly 400 applied to a foot 502 of a patient. FIG. 5B is a top view of the wound-care assembly 400 applied to a foot 502 of a patient. As illustrated in FIGS. 5A-5B a wound 504 is present on the foot 502. The wound 504 is illustrated by way of example in FIG. 5 as being present on the foot 502; however, in other embodiments, the wound 504 may be disposed on any bodily region of the patient. The fiber-optic patch 402 is positioned over the wound 504 in such a manner that the fiber-optic strands 404 extend across a width of the wound 504. A fluid conductor 506 is shaped to approximately match a shape of the wound 504. In a typical embodiment, the fluid conductor 506 is flexible, absorptive, and constructed of, for example, medical grade foam. The fluid conductor 506 may cut or otherwise shaped to approximately match a size and shape of the wound 504. The fluid conductor 506 is positioned above the fiber-optic patch 402 and pressed downwardly into the wound 504 thereby pressing the fiber-optic strands 404 into contact with an interior surface of the wound 504. In various embodiments, a straw portion 508 may be fluidly coupled to the fluid conductor 506. In a typical embodiment, the straw portion 508 is constructed from a material similar to that of the fluid conductor 506. The straw portion 508 allows a relative vacuum to be applied to the wound 504, via the vacuum applicator 408, when the fluid port 410 is disposed a location remote to the wound 504 such as, for example, on a top of the foot 502. Such an arrangement is advantageous in situations where the wound 504 is located in a space-confined area such as, for example, a bottom of the patient's foot 502. The fiber-optic patch 402, the fluid conductor 506, and the straw portion 508 are secured in place via a biocompatible skin adhesive such as, for example, tegaderm.

Still referring to FIGS. 5A-5B, a small hole is formed in the biocompatible skin adhesive at a location where the vacuum applicator 408 is to be applied. In various embodiments, the vacuum applicator 408 is applied above the fluid conductor 506; however, in other embodiments, the vacuum applicator 408 may be applied to the straw portion 508. The vacuum applicator 408 is secured via a biocompatible skin adhesive such as, for example, tegaderm. In a typical embodiment, the wound-care assembly 400 facilitates flexible and modular construction for use on a wide variety of bodily areas and wound types.

FIG. 6 is a flow diagram of a process 600 for using the wound-care patch 400. The process 600 starts at step 602. At step 604, the fiber-optic patch 402 is placed over the wound 504. At step 606, the fluid conductor 506 is sized to approximately match a size and shape of the wound 504. At step 608, the fluid conductor 506 is pressed into the wound 504 above the fiber-optic patch 402. The fluid conductor 506 presses the fiber-optic strands 404 into contact with an inner surface of the wound 504. At step 610, a straw portion 508 is constructed in fluid communication with the fluid conductor 506. At step 612, the fiber-optic patch 402, the fluid conductor 506, and the straw portion 508 are secured with a biocompatible skin adhesive such as, for example, tegaderm. At step 614, the vacuum applicator is applied to at least one of the straw portion 508 or the fluid conductor 506.

Still referring to FIG. 6, at step 616, the fiber-optic cable 406 is connected to a source of ultraviolet light and the vacuum applicator 408 is fluidly coupled to a vacuum source. At step 618, a relative vacuum is applied to the wound 504 via the vacuum applicator 408, the fluid conductor 506, and, in some embodiments, the straw portion 508. In various embodiments, the relative vacuum facilitates removal undesirable tissues from the wound 504. At step 620, ultraviolet light is applied to the wound 504 via the fiber-optic cable 406, the fiber-optic patch 402, and the fiber-optic strands 404. In a typical embodiment, the ultraviolet light is supplied to the wound 504 simultaneous with the application of the relative vacuum. In other embodiments, at least one of the ultraviolet light and the relative vacuum may be modulated or applied in various patterns and, thus, may not be simultaneous. The process 600 ends at step 622.

Although various embodiments of the method and system of the present invention have been illustrated in the accompanying Drawings and described in the foregoing Specification, it will be understood that the invention is not limited to the embodiments disclosed, but is capable of numerous rearrangements, modifications, and substitutions without departing from the spirit and scope of the invention as set forth herein. It is intended that the Specification and examples be considered as illustrative only. 

What is claimed is:
 1. A wound-care assembly comprising: a base layer; a film layer operatively coupled to the base layer; a fluid conductor in fluid communication with a wound and a vacuum source, the fluid conductor being sized to fit inside the wound; a fiber-optic patch comprising a plurality of fiber-optic strands, the fiber-optic strands being pressed and secured into contact with an interior surface of the wound by the fluid conductor; wherein the fiber-optic patch provides ultraviolet light to the wound; and wherein a relative vacuum is applied to the wound via the vacuum source and the fluid conductor.
 2. The wound-care assembly of claim 1, further comprising a fluid port fluidly coupled to the fluid conductor.
 3. The wound-care assembly of claim 2, wherein the fluid conductor comprises a straw portion that facilitates placement of the fluid port at a location distal to the wound.
 4. The wound-care assembly of claim 2, wherein a therapeutic agent is applied to the wound via the fluid port.
 5. The wound-care assembly of claim 4, wherein the therapeutic agent is thermally augmented.
 6. The wound-care assembly of claim 1, wherein the fiber-optic strands are arranged in a flat, side-by-side, configuration.
 7. The wound-care assembly of claim 1, further comprising a window formed in the base layer, the window facilitating fluid communication between the wound and the fluid conductor.
 8. The wound-care assembly of claim 7, further comprising a mesh extending across the window.
 9. The wound-care assembly of claim 7, further comprising a radio-frequency (RF) antenna disposed around a circumference of the window.
 10. The wound-care assembly of claim 1, wherein the fluid conductor facilitates reduction of pressure at the wound from ambient pressure.
 11. A method of utilizing a wound-care assembly, the method comprising: applying a fiber-optic patch to a wound; sizing a fluid conductor to fit inside the wound; pressing and securing the fiber-optic patch into contact with an inner surface of the wound via the fluid conductor; applying a vacuum applicator to the fluid conductor; applying ultraviolet light to the wound via the fiber-optic patch; and applying a relative vacuum to the wound via the fluid conductor.
 12. The method of claim 11, further comprising securing the fluid conductor and the fiber-optic patch to the wound.
 13. The method of claim 11, further comprising applying a therapeutic agent to the wound via the fluid conductor.
 14. The method of claim 13, further comprising thermally augmenting the therapeutic agent.
 15. The method of claim 11, further comprising applying a pulsed radio-frequency (RF) signal to the wound via a radio-frequency antenna.
 16. The method of claim 11, wherein applying ultraviolet light comprises modulating the applied ultraviolet light.
 17. The method of claim 11, wherein applying a relative vacuum comprises fluidly coupling the vacuum applicator to a straw portion of the fluid conductor at a location distal to the wound.
 18. The method of claim 11, further comprising shaping the fluid conductor to approximately match a size and a shape of the wound.
 19. The method of claim 11, wherein applying a relative vacuum to a wound facilitates removal of undesirable materials from the wound.
 20. The method of claim 11, wherein the fiber-optic patch comprises fiber-optic strands arranged in a flat side-by-side configuration. 